Patent classifications
C08G18/78
INNOVATIVE HYDROPHILIC POLYISOCYANATES WITH IMPROVED STORAGE STABILITY
The invention relates to innovative, water-dispersible, hydrophilic polyisocyanates and polyisocyanate mixtures, to a process for preparing them, to compositions comprising the hydrophilic polyisocyanates of the invention, and to their use as a starting component in the production of polyurethane plastics, more particularly as crosslinkers for water-soluble or water-dispersible film-forming, adhesives or sealant binders or binder components having groups which are reactive towards isocyanate groups.
One-pack moisture-curing composition
A one-pack moisture-curing composition of the present technology contains a preliminary composition, an adhesiveness-imparting agent containing a compound (A) and/or a compound (B), a first catalyst containing a compound (C) and/or dibutyltin bis(pentadione), and a second catalyst containing a dimorpholinodiethylether.
ONE PART, CATALYST CONTAINING, MOISTURE CURABLE DUAL CURE RESINS FOR ADDITIVE MANUFACTURING
Provided is method of making a three-dimensional object comprising polyurea, which may include: (a) dispensing a one part (1K) dual cure resin into a stereolithography apparatus, the resin comprising or consisting essentially of a photoinitiator, a reactive blocked polyisocyanate, optionally a catalyst such as a polyurethane blowing catalyst, and optionally a polyepoxide; (b) additively manufacturing from said resin an intermediate object comprising the light polymerization product of said reactive blocked polyisocyanate; (c) optionally cleaning said intermediate object; and (d) reacting said polymerization product in said intermediate with water in the presence of a catalyst such as a polyurethane blowing catalyst (which may be included in the resin, the water, or both) to generate polyamine in situ that sequentially reacts with the remainder of the polymerization product to form urea linkages and thereby produce a three-dimensional object comprising polyurea. Dual cure resins useful for the method are also provided.
Waterborne azido-alkyne click compositions
A waterborne alternative polyurethane composition is provided which comprises a reaction product of: an azidated polyol; and a waterborne poly(alkynyl carbamate) prepolymer comprising a reaction product of a polyisocyanate and from 1 wt. % to 20 wt. % of an alkynol-polyether having a formula (I),
R.sub.1—R.sub.2—O—R.sub.3—OH (I),
wherein, R.sub.1=a monovalent group selected from either HC≡C— or HC≡C—CO—, R.sub.2=a divalent alkylene group from 1 to 8 carbon atoms, and may be straight chain or branched and may contain cyclic moieties, and R.sub.3=a polyethylene glycol with number average molecular weight from 300-1,200 g/mol, wherein the wt. % is based on the weight of the prepolymer, wherein reaction of the azidated polyol and the waterborne poly(alkynyl carbamate) occurs at a temperature of from 20° C. to 200° C. and optionally in the presence of a catalyst. The inclusion of an alkynol-polyether does not materially alter the performance properties and reactivity of the waterborne polyurethane composition relative to a solventborne polyurethane control composition. Inclusion of the alkynol-polyether reduces the need for organic solvents by allowing for the use of water as a carrier. The inventive waterborne alternative polyurethane compositions may find use in or as coatings, adhesives, sealants, films, elastomers, castings, foams, and composites.
POLYURETHANE WITH (2-OXO-1,3-DIOXOLANE-4-CARBOXYLATE) END GROUPS
The present invention relates to a polyurethane (PP2) comprising at least two, preferably two or three, end functional groups T of following formula (I):
##STR00001##
The present invention also relates to the uses of the polyurethanes (PP2) for the preparation of multicomponent systems.
Process for continuous isocyanate modification
A process for continuous preparation of oligomeric or polymeric isocyanates by catalytic modification of monomeric di- and/or triisocyanates, characterized in that at least one isocyanate component A and at least one catalyst component B are combined continuously in a reaction apparatus and conducted through the reaction apparatus as a reaction mixture, the residence time distribution being characterized according to the dispersion model by Bo (Bodenstein number) above 40, preferably above 60 and most preferably above 80.
Flame resistant flexible polyurethane foam
A method of forming a flame resistant flexible polyurethane foam that has a V-0 rating, according to Underwriters Laboratories Standard 94 Flammability Test, includes forming a reaction mixture that has an isocyanate component and an isocyanate-reactive component, and the isocyanate-reactive component includes a polyol component. The isocyanate component includes at least 30 wt % of a biuret modified aromatic diisocyanate, based on a total weight of the isocyanate component, and an isocyanate index of the reaction mixture is less than 100. The polyol component includes at least 5 wt % of a filled polyether polyol and at least 65 wt % of one or more other polyols that are different from the filled polyether polyol, based on a total weight of the isocyanate-reactive component.
Flame resistant flexible polyurethane foam
A method of forming a flame resistant flexible polyurethane foam that has a V-0 rating, according to Underwriters Laboratories Standard 94 Flammability Test, includes forming a reaction mixture that has an isocyanate component and an isocyanate-reactive component, and the isocyanate-reactive component includes a polyol component. The isocyanate component includes at least 30 wt % of a biuret modified aromatic diisocyanate, based on a total weight of the isocyanate component, and an isocyanate index of the reaction mixture is less than 100. The polyol component includes at least 5 wt % of a filled polyether polyol and at least 65 wt % of one or more other polyols that are different from the filled polyether polyol, based on a total weight of the isocyanate-reactive component.
Polymerisable plasticiser, liquid polyurethane resin composition comprising same and uses thereof
The present invention relates to a polymerisable plasticiser formed by a hydrocarbon chain, one end of which bears more than one isocyanate function, said hydrocarbon chain comprising and/or being substituted by an aromatic ring and/or an aliphatic ring and/or said hydrocarbon chain is substituted by at least two hydrocarbon chains that can comprise an unsaturation, and the number of isocyanate functions being strictly greater than 1, preferably greater than 1.2, and, more preferably, grater than 1.5 but less than or equal to 2.2. The invention also relates to liquid polyurethane resin compositions and, in particular, stable, ready-to-use liquid polyurethane resin compositions comprising said plasticiser. The invention further relates to methods for replacing all or part of the exogenous plasticiser and/or solvent in a polyurethane resin by adding said polymerisable plasticiser.
Urethane acrylates for curable coatings
A urethane (meth)acrylate not comprising caprolactone is the product of reaction of A) a monoalcohol bearing from 1 to 5 (meth)acrylates, B) an allophanate-modified polyisocyanate, C) optionally, in the presence of a saturated polyol of functionality 2 to 3, D) optionally, in the presence of an unsaturated polyol with a hydroxyl functionality of 2 to 4, said polyol being C.sub.3 to C.sub.18, E) optionally, in the presence of a reactive diluent. A process for preparing the urethane (meth)acrylate includes reacting the monoalcohol A) and the polyisocyanate B) in the optional presence of C), D), and/or E). The urethane (meth)acrylate may be used in curable compositions for coatings, in particular for varnishes and inks, adhesives, adhesion primers, coatings for wood, metal or plastic and application by spray gun and provide a good compromise between reactivity, flexibility, adherence, hardness, and ease of use.